Covalent Walk-In QC, Production & Regulatory
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs
- Quality Control
- Production
- Production Documentation
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience:
- Required Skills:
- Location & Salary
- Job Location:
- Salary:
- Benefits:
- Application Process
- Walk-In Details:
- Documents to Carry:
- Contact Details:
- Why This Opportunity Matters
- Frequently Asked Questions (FAQs)
- 1. Can freshers apply?
- 2. What is the interview mode?
- 3. What qualifications are required?
- 4. Are there employee benefits?
- 5. How can I apply?
- Summary
Covalent Laboratories Private Limited is conducting a walk-in interview for multiple vacancies across Regulatory Affairs, Quality Control, Production, and Production Documentation at its Sangareddy facility. This hiring drive is open to freshers and experienced candidates with 0 to 5 years of experience, offering a strong entry point into a WHO-GMP, USFDA, and EU-GMP approved pharmaceutical manufacturing environment. The walk-in will be held on 13th and 14th April 2026, making it an immediate opportunity for candidates seeking pharma jobs in Telangana.
Company Overview
Covalent Laboratories Private Limited is a well-established pharmaceutical company with certifications including ISO 14001, WHO-GMP, USFDA, and EU-GMP approvals. The company is known for its compliance-driven manufacturing practices and strong presence in regulated markets.
With a focus on quality, environmental responsibility, and global regulatory standards, Covalent Laboratories provides professionals with exposure to advanced pharmaceutical manufacturing systems and compliance frameworks. The organization continues to expand its footprint in API and formulation segments, making it a reliable platform for career growth.
Job Role & Responsibilities
Regulatory Affairs
- Assist in preparation and submission of regulatory dossiers
- Ensure compliance with international regulatory guidelines
- Maintain documentation for approvals and audits
Quality Control
- Perform analysis of raw materials, intermediates, and finished products
- Operate analytical instruments and maintain lab records
- Follow GLP and data integrity practices
Production
- Execute manufacturing operations as per SOPs
- Handle equipment and ensure process compliance
- Maintain batch records and production documentation
Production Documentation
- Prepare and review batch manufacturing records
- Ensure accuracy and compliance in documentation
- Support audits and quality checks
Eligibility / Qualifications
Educational Qualification:
M.Sc Organic Chemistry, M.Sc Analytical Chemistry, B.Sc, B.Pharmacy, M.Pharmacy
Relevant Courses:
B.Sc Chemistry, M.Sc Organic Chemistry, M.Sc Analytical Chemistry, B.Pharmacy, M.Pharmacy
Experience:
- Regulatory Affairs: 0–4 Years
- Quality Control: 0–5 Years
- Production: 1–5 Years
- Production Documentation: 0–4 Years
Required Skills:
- Knowledge of GMP, GLP, and regulatory compliance
- Strong documentation and data handling skills
- Basic understanding of pharmaceutical manufacturing processes
- Ability to work in a regulated environment
Location & Salary
Job Location:
Gundla Machnoor, Sangareddy, Telangana
Salary:
Not disclosed (as per company norms)
Benefits:
- Subsidized canteen
- Attendance bonus
- Free transportation
Application Process
Candidates can directly attend the walk-in interview with required documents.
Walk-In Details:
- Dates: 13th & 14th April 2026
- Venue: Covalent Laboratories, Gundla Machnoor, Sangareddy
Documents to Carry:
- Updated resume
- Educational documents
- ID proof
Contact Details:
- Phone: 9100132004, 9100167917
- Email: hr@covalentlab.com
Why This Opportunity Matters
This walk-in drive offers an excellent opportunity for both freshers and experienced candidates to enter a globally approved pharmaceutical company. Exposure to regulated manufacturing environments and compliance systems helps build a strong foundation in pharma careers.
Frequently Asked Questions (FAQs)
1. Can freshers apply?
Yes, freshers can apply for Regulatory Affairs, QC, and Documentation roles.
2. What is the interview mode?
Walk-in interview at the Sangareddy location.
3. What qualifications are required?
B.Sc, M.Sc, B.Pharmacy, and M.Pharmacy candidates are eligible.
4. Are there employee benefits?
Yes, canteen, transportation, and attendance bonus are provided.
5. How can I apply?
Attend the walk-in or contact HR via phone or email.
Summary
| Company | Covalent Laboratories Pvt. Ltd. |
|---|---|
| Vacancies | QC Analyst, Production Executive, Regulatory Associate, Documentation Officer |
| Required Education | B.Sc, M.Sc, B.Pharmacy, M.Pharmacy |
| Experience | 0–5 Years |
